K-Wire, 1.35 mm x 170 mm
Reported: May 11, 2022 Initiated: March 25, 2022 #Z-1035-2022
Product Description
K-Wire, 1.35 mm x 170 mm
Reason for Recall
Products do not meet length and diameter specifications.
Details
- Recalling Firm
- Arthrex, Inc.
- Units Affected
- 300 pieces
- Distribution
- Worldwide distribution - US Nationwide distribution in the states of OH, TN, MO, LA, IA, AZ, PA, NY, OR and the countries of to Belgium, Egypt, Finland, France, Germany, Italy, Netherlands, Norway, Poland, Portugal, and Spain.
- Location
- Naples, FL
Frequently Asked Questions
What product was recalled? ▼
K-Wire, 1.35 mm x 170 mm. Recalled by Arthrex, Inc.. Units affected: 300 pieces.
Why was this product recalled? ▼
Products do not meet length and diameter specifications.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on May 11, 2022. Severity: Moderate. Recall number: Z-1035-2022.
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